CO6270223A2 - DERIVATIVES OF PIRIDIN-2-ILAMINO-1,2,4 TIADIAZOL AS GLUCOCINASE ACTIVATORS FOR THE TREATMENT OF MELLITUS DIABETES - Google Patents
DERIVATIVES OF PIRIDIN-2-ILAMINO-1,2,4 TIADIAZOL AS GLUCOCINASE ACTIVATORS FOR THE TREATMENT OF MELLITUS DIABETESInfo
- Publication number
- CO6270223A2 CO6270223A2 CO10046631A CO10046631A CO6270223A2 CO 6270223 A2 CO6270223 A2 CO 6270223A2 CO 10046631 A CO10046631 A CO 10046631A CO 10046631 A CO10046631 A CO 10046631A CO 6270223 A2 CO6270223 A2 CO 6270223A2
- Authority
- CO
- Colombia
- Prior art keywords
- treatment
- tiadiazol
- piridin
- ilamino
- derivatives
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Se proporcionan compuestos de la Formula Ien donde R2, R3, R13, L y D2 son lo definido en la memoria descriptiva, que son ·tiles en el tratamiento y/o en la prevencion de enfermedades o trastornos mediados por niveles deficientes de actividad de glucocinasa o que se pueden tratar activando glucocinasa que incluyen, en forma no taxativa, diabetes mellitus, deterioro de tolerancia de la glucosa, IFG (deterioro de glucosa en ayunas) e IFG (deterioro de glucemia en ayunas), asi como otras enfermedades y trastornos tales como aquellos discutidos en la presente.Formula I compounds are provided where R2, R3, R13, L and D2 are defined in the specification, which are useful in the treatment and / or in the prevention of diseases or disorders mediated by deficient levels of glucokinase activity or that can be treated by activating glucokinase that include, non-taxatively, diabetes mellitus, impaired glucose tolerance, IFG (impaired fasting glucose) and IFG (impaired fasting blood glucose), as well as other diseases and disorders such like those discussed in the present.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97422507P | 2007-09-21 | 2007-09-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO6270223A2 true CO6270223A2 (en) | 2011-04-20 |
Family
ID=40250949
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO10046631A CO6270223A2 (en) | 2007-09-21 | 2010-04-21 | DERIVATIVES OF PIRIDIN-2-ILAMINO-1,2,4 TIADIAZOL AS GLUCOCINASE ACTIVATORS FOR THE TREATMENT OF MELLITUS DIABETES |
Country Status (29)
Country | Link |
---|---|
US (3) | US8212045B2 (en) |
EP (4) | EP2209778B1 (en) |
JP (1) | JP5722037B2 (en) |
KR (1) | KR101566042B1 (en) |
CN (1) | CN101868459B (en) |
AR (1) | AR068628A1 (en) |
AU (1) | AU2008305294B2 (en) |
BR (1) | BRPI0816881A2 (en) |
CA (1) | CA2699718C (en) |
CO (1) | CO6270223A2 (en) |
CR (2) | CR11383A (en) |
DK (1) | DK2209778T3 (en) |
EA (1) | EA019104B1 (en) |
ES (2) | ES2393824T3 (en) |
HK (2) | HK1145498A1 (en) |
HR (1) | HRP20120814T1 (en) |
IL (1) | IL204264A (en) |
MA (1) | MA31779B1 (en) |
MX (1) | MX2010002772A (en) |
MY (1) | MY180558A (en) |
NZ (1) | NZ583538A (en) |
PL (1) | PL2209778T3 (en) |
PT (1) | PT2209778E (en) |
SI (1) | SI2209778T1 (en) |
TN (1) | TN2010000100A1 (en) |
TW (1) | TWI423799B (en) |
UA (1) | UA101166C2 (en) |
WO (1) | WO2009042435A1 (en) |
ZA (2) | ZA201002206B (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008061108A2 (en) * | 2006-11-15 | 2008-05-22 | Forest Laboratories Holdings Limited | Phthalazine derivatives |
PT2209778E (en) | 2007-09-21 | 2012-12-06 | Array Biopharma Inc | Pyridin-2 -yl-amino-i, 2, 4 -thiadiazole derivatives as glucokinase activators for the treatment of diabetes mellitus |
WO2011107494A1 (en) | 2010-03-03 | 2011-09-09 | Sanofi | Novel aromatic glycoside derivatives, medicaments containing said compounds, and the use thereof |
ES2624780T3 (en) | 2010-03-31 | 2017-07-17 | The Scripps Research Institute | Cell reprogramming |
US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
CA2808590A1 (en) | 2010-08-23 | 2012-03-01 | Amgen Inc. | Sulfonylpiperazine derivatives that interact with glucokinase regulatory protein for the treatment of diabetes |
EP2684878A4 (en) | 2011-03-09 | 2014-08-27 | Daiichi Sankyo Co Ltd | Dipyridylamine derivative |
CA2832286A1 (en) | 2011-04-05 | 2012-10-11 | Amgen Inc. | Benzodioxepine and benzodioxine compounds that interact with glucokinase regulatory protein for the treatment of diabetes |
WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
WO2013123444A1 (en) | 2012-02-17 | 2013-08-22 | Amgen Inc. | Sulfonyl compounds that interact with glucokinase regulatory protein |
WO2013173382A1 (en) | 2012-05-15 | 2013-11-21 | Amgen Inc. | Benzothiophene sulfonamides and other compounds that interact with glucokinase regulatory protein |
WO2013173672A1 (en) | 2012-05-18 | 2013-11-21 | Array Biopharma Inc. | Method for the preparation of thiadiazoles |
CA2890852A1 (en) * | 2012-11-09 | 2014-05-15 | Array Biopharma Inc. | Crystalline forms of (1s)-1-[5-({3-[(2-methylpyridin-3-yl)oxy]-5-(pyridin-2-ylsulfanyl)pyridin-2-yl}amino)-1,2,4-thiadiazol-3-yl]ethane-1,2-diol |
WO2016059647A2 (en) * | 2014-10-13 | 2016-04-21 | SHRI CHHATRAPTI SHIVAJI COLLEGE Maharashtra, India) | Triaminotriazine picolinonitrile derivatives as potent reverse transcriptase inhibitor of hiv-1 |
GB201714777D0 (en) | 2017-09-14 | 2017-11-01 | Univ London Queen Mary | Agent |
CN111372579B (en) | 2017-10-30 | 2023-08-22 | 神经孔疗法股份有限公司 | Substituted phenylsulfonyl phenyltriazolethiones and use thereof |
MX2020012969A (en) * | 2018-05-31 | 2021-02-16 | Hua Medicine Shanghai Ltd | Pharmaceutical combination and composition, and combination preparation containing glucokinase activator and biguanide hypoglycemic drug as well as preparation method and use thereof. |
Family Cites Families (82)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3983246A (en) | 1974-04-04 | 1976-09-28 | Fmc Corporation | N-(sulfonyloxy) benzimidoyl halides as bactericidal or fungicidal agents |
DE2949913A1 (en) * | 1979-12-12 | 1981-06-25 | Basf Ag, 6700 Ludwigshafen | AZO DYES |
EP0300688A1 (en) | 1987-07-21 | 1989-01-25 | FISONS plc | Pyrrole derivatives, process for their preparation and pharmaceutical compositions containing them |
JPH0228168A (en) * | 1988-04-14 | 1990-01-30 | Sankyo Co Ltd | Thiazole derivative |
US5326776A (en) * | 1992-03-02 | 1994-07-05 | Abbott Laboratories | Angiotensin II receptor antagonists |
WO1993024442A1 (en) | 1992-05-29 | 1993-12-09 | Yamanouchi Pharmaceutical Co., Ltd. | Medicine containing benzoic acid derivative and novel benzoic acid derivative |
EP0766676B1 (en) | 1994-06-24 | 2002-05-22 | Euroceltique S.A. | Compounds for inhibiting phosphodiesterase iv |
GB9908410D0 (en) * | 1999-04-13 | 1999-06-09 | Pfizer Ltd | Pyridines |
IL144910A0 (en) * | 1999-04-15 | 2002-06-30 | Bristol Myers Squibb Co | Cyclic compounds and pharmaceutical compositions containing the same |
US7125875B2 (en) | 1999-04-15 | 2006-10-24 | Bristol-Myers Squibb Company | Cyclic protein tyrosine kinase inhibitors |
NZ515086A (en) | 1999-04-28 | 2003-10-31 | Aventis Pharma Gmbh | Di-aryl acid derivatives as PPAR receptor ligands |
KR100722090B1 (en) | 1999-05-21 | 2007-05-25 | 바이오비트럼 에이비 | Novel compounds, their use and preparation |
US6465467B1 (en) * | 1999-05-21 | 2002-10-15 | Biovitrum Ab | Certain aryl-aliphatic and heteroaryl-aliphatic piperazinyl pyrazines and their use in the treatment of serotonin-related diseases |
JP4144978B2 (en) | 1999-09-09 | 2008-09-03 | 富士フイルム株式会社 | Synthesis method of 1,2,4-thiadiazole derivatives |
EP1218376B1 (en) * | 1999-09-10 | 2005-11-09 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
US20020065270A1 (en) | 1999-12-28 | 2002-05-30 | Moriarty Kevin Joseph | N-heterocyclic inhibitors of TNF-alpha expression |
WO2001047921A1 (en) | 1999-12-28 | 2001-07-05 | Pharmacopeia, Inc. | Pyrimidine and triazine kinase inhibitors |
US6906067B2 (en) | 1999-12-28 | 2005-06-14 | Bristol-Myers Squibb Company | N-heterocyclic inhibitors of TNF-α expression |
US7345051B2 (en) | 2000-01-31 | 2008-03-18 | Genaera Corporation | Mucin synthesis inhibitors |
JP2004507526A (en) | 2000-08-31 | 2004-03-11 | ファイザー・プロダクツ・インク | Pyrazole derivatives and their use as protein kinase inhibitors |
US20050209297A1 (en) * | 2000-08-31 | 2005-09-22 | Pfizer Inc | Pyrazole derivatives |
WO2002030357A2 (en) | 2000-10-11 | 2002-04-18 | Chemocentryx, Inc. | Compounds and methods for modulating ccr4 function |
AU2002213467A1 (en) | 2000-10-11 | 2002-04-22 | Chemocentryx, Inc. | Modulation of ccr4 function |
JP2004521878A (en) | 2000-12-07 | 2004-07-22 | スィーヴィー セラピューティクス インコーポレイテッド | Compounds that increase ABCA-1 |
AU2002234047A1 (en) | 2000-12-21 | 2002-07-01 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
WO2002064096A2 (en) | 2001-02-16 | 2002-08-22 | Tularik Inc. | Methods of using pyrimidine-based antiviral agents |
WO2002094264A1 (en) * | 2001-05-23 | 2002-11-28 | Tularik Inc. | Ccr4 antagonists |
EP1397142A4 (en) | 2001-06-19 | 2004-11-03 | Bristol Myers Squibb Co | Pyrimidine inhibitors of phosphodiesterase (pde) 7 |
PE20030008A1 (en) | 2001-06-19 | 2003-01-22 | Bristol Myers Squibb Co | DUAL INHIBITORS OF PDE 7 AND PDE 4 |
WO2003000687A1 (en) * | 2001-06-22 | 2003-01-03 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
JP4505228B2 (en) | 2002-01-10 | 2010-07-21 | バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト | Rho-kinase inhibitor |
WO2003066099A1 (en) | 2002-02-05 | 2003-08-14 | Yamanouchi Pharmaceutical Co., Ltd. | 2,4,6-triamino-1,3,5-triazine derivative |
ATE466580T1 (en) * | 2002-03-15 | 2010-05-15 | Vertex Pharma | AZOLYLAMINOAZINE AS PROTEIN KINASE INHIBITORS |
WO2003078423A1 (en) | 2002-03-15 | 2003-09-25 | Vertex Pharmaceuticals, Inc. | Compositions useful as inhibitors of protein kinases |
EP1485381B8 (en) * | 2002-03-15 | 2010-05-12 | Vertex Pharmaceuticals Incorporated | Azolylaminoazine as inhibitors of protein kinases |
ATE468336T1 (en) | 2002-03-15 | 2010-06-15 | Vertex Pharma | AZOLYLAMINOAZINE AS PROTEIN KINASE INHIBITORS |
IL164302A0 (en) * | 2002-03-29 | 2005-12-18 | Chiron Corp | Substituted benzazoles and use thereof as raf kinase inhibitors |
US8299108B2 (en) * | 2002-03-29 | 2012-10-30 | Novartis Ag | Substituted benzazoles and methods of their use as inhibitors of raf kinase |
JPWO2003091213A1 (en) * | 2002-04-25 | 2005-09-02 | アステラス製薬株式会社 | Novel amide derivative or salt thereof |
US7015227B2 (en) * | 2002-06-21 | 2006-03-21 | Cgi Pharmaceuticals, Inc. | Certain amino-substituted monocycles as kinase modulators |
US20040132726A1 (en) * | 2002-08-09 | 2004-07-08 | Astrazeneca Ab And Nps Pharmaceuticals, Inc. | New compounds |
WO2004024159A1 (en) | 2002-09-10 | 2004-03-25 | Scios Inc. | INHIBITORS OF TFGβ |
AU2003302279B2 (en) | 2002-10-03 | 2008-06-12 | Novartis Ag | Substituted (thiazol-2-yl) -amide or sulfonamide as glycokinase activators useful in the treatment of Type 2 diabetes |
AU2003285007A1 (en) | 2002-10-30 | 2004-06-07 | Merck & Co., Inc. | Kinase inhibitors |
CN101723891A (en) | 2003-02-10 | 2010-06-09 | 沃泰克斯药物股份有限公司 | Processes for the preparation of N-heteroaryl-N-aryl-amines by reacting an N-aryl carbamic acid ester with a halo-heteroaryl and analogous processes |
US20040248850A1 (en) * | 2003-02-11 | 2004-12-09 | Kemia, Inc. | Compounds for the treatment of HIV infection |
PE20050194A1 (en) * | 2003-02-13 | 2005-04-23 | Banyu Pharma Co Ltd | PYRIDINE-2-CARBOXAMIDE DERIVATIVES AS GLUCOKINASE ACTIVATORS |
CA2523126A1 (en) | 2003-03-25 | 2004-10-14 | Vertex Pharmaceuticals Incorporated | Thiazoles useful as inhibitors of protein kinases |
US7244763B2 (en) * | 2003-04-17 | 2007-07-17 | Warner Lambert Company Llc | Compounds that modulate PPAR activity and methods of preparation |
CN1845915A (en) * | 2003-09-02 | 2006-10-11 | 默克公司 | Bipyridyl amines and ethers as modulators of metabotropic glutamate receptor-5 |
US7470712B2 (en) | 2004-01-21 | 2008-12-30 | Bristol-Myers Squibb Company | Amino-benzazoles as P2Y1 receptor inhibitors |
WO2005077373A2 (en) | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Treatment of gastro-esophageal reflux disease (gerd) |
AR049418A1 (en) | 2004-02-27 | 2006-08-02 | Bayer Pharmaceuticals Corp | DERIVATIVES OF HETEROARILAMINOPIRAZOL AND PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF DIABETES. |
KR20050091462A (en) | 2004-03-12 | 2005-09-15 | 한국과학기술연구원 | Furopyrimidine compound and ddr2 tyrosine kinase activity inhibitor comprising the same |
WO2005090332A1 (en) | 2004-03-23 | 2005-09-29 | Banyu Pharmaceutical Co., Ltd | Substituted quinazoline or pyridopyrimidine derivative |
US7781451B2 (en) * | 2004-04-02 | 2010-08-24 | Novartis Ag | Thiazolopyridine derivatives, pharmaceut ical conditions containing them and methods of treating glucokinase mediated conditions |
US20080108600A1 (en) | 2004-04-13 | 2008-05-08 | Icagen, Inc. | Polycyclic Pyridines as Potassium Ion Channel Modulators |
ATE458730T1 (en) | 2004-04-13 | 2010-03-15 | Icagen Inc | POLYCYCLIC PYRAZINE AS POTASSIUM ION CHANNEL MODULATORS |
TW200606129A (en) * | 2004-07-26 | 2006-02-16 | Chugai Pharmaceutical Co Ltd | Novel cyclohexane derivative, its prodrug, its salt and diabetic therapeutic agent containing the same |
JP2008526734A (en) | 2004-12-31 | 2008-07-24 | エスケー ケミカルズ カンパニー リミテッド | Quinazoline derivatives effective in preventing diabetes and obesity |
WO2006078621A2 (en) | 2005-01-19 | 2006-07-27 | Bristol-Myers Squibb Company | 2-phenoxy-n- (1, 3 , 4-thiadizol-2-yl) pyridin-3-amine derivatives and related compounds as p2y1 receptor inhibitors for the treatment of thromboembolic disorders |
DE102005025161A1 (en) | 2005-06-01 | 2006-12-07 | Phenion Gmbh & Co. Kg | New pyrimidine- and triazine derivatives are peroxisome proliferator activated receptor modulators, useful to treat e.g. diabetes, insulin resistance, obesity, hyperlipidemia, cardiovascular diseases and Alzheimer's disease |
EP1917259B1 (en) | 2005-08-18 | 2012-01-25 | Vertex Pharmaceuticals Incorporated | Pyrazine kinase inhibitors |
BRPI0615236A2 (en) * | 2005-08-31 | 2011-05-10 | Astellas Pharma Inc | thiazole derivative |
WO2007038387A2 (en) | 2005-09-23 | 2007-04-05 | Yale University | Compounds and methods for the treatment of viruses and cancer |
JP5137207B2 (en) | 2005-11-01 | 2013-02-06 | アレイ バイオファーマ、インコーポレイテッド | Glucokinase activator |
NZ606259A (en) | 2005-11-03 | 2014-06-27 | Vertex Pharma | Aminopyrimidines useful as kinase inhibitors |
CA2629781A1 (en) * | 2005-11-16 | 2007-05-24 | Vertex Pharmaceuticals Incorporated | Aminopyrimidines useful as kinase inhibitors |
WO2007058482A1 (en) | 2005-11-16 | 2007-05-24 | Lg Life Sciences, Ltd. | Novel inhibitors of protein kinase |
EP1986645B1 (en) | 2006-01-27 | 2012-01-04 | Array Biopharma, Inc. | Glucokinase activators |
KR101440634B1 (en) * | 2006-03-24 | 2014-09-22 | 어레이 바이오파마 인크. | 2-aminopyridine analogs as glucokinase activators |
WO2007131953A1 (en) | 2006-05-12 | 2007-11-22 | Ab Science | A new process for the synthesis of 2-aminoxazole compounds |
US20080076800A1 (en) | 2006-08-24 | 2008-03-27 | Huang Kenneth H | Benzene, Pyridine, and Pyridazine Derivatives |
TW200825060A (en) | 2006-10-26 | 2008-06-16 | Astrazeneca Ab | Chemical compounds |
ME00811B (en) | 2006-12-08 | 2012-03-20 | Novartis Ag | Compounds and compositions as protein kinase inhibitors |
US8431713B2 (en) | 2007-01-24 | 2013-04-30 | Array Biopharma, Inc. | 2-aminopyridine derivatives as glucokinase activators |
EP2173745A2 (en) * | 2007-03-23 | 2010-04-14 | Array Biopharma, Inc. | 2-aminopyridine analogs as glucokinase activators |
ES2470341T3 (en) | 2007-04-05 | 2014-06-23 | Amgen, Inc | Aurora kinase modulators and method of use |
US20090012091A1 (en) | 2007-07-02 | 2009-01-08 | Kinagen, Inc. | Oximide derivatives and their therapeutical application |
WO2009022171A1 (en) | 2007-08-13 | 2009-02-19 | Astrazeneca Ab | Pyridinyiioxy pyridines as alk5 inhibitors |
PT2209778E (en) | 2007-09-21 | 2012-12-06 | Array Biopharma Inc | Pyridin-2 -yl-amino-i, 2, 4 -thiadiazole derivatives as glucokinase activators for the treatment of diabetes mellitus |
SI2195312T1 (en) | 2007-10-09 | 2013-01-31 | Merck Patent Gmbh | Pyridine derivatives useful as glucokinase activators |
-
2008
- 2008-09-15 PT PT88345046T patent/PT2209778E/en unknown
- 2008-09-15 BR BRPI0816881 patent/BRPI0816881A2/en not_active IP Right Cessation
- 2008-09-15 AU AU2008305294A patent/AU2008305294B2/en not_active Ceased
- 2008-09-15 MY MYPI2010001186A patent/MY180558A/en unknown
- 2008-09-15 NZ NZ583538A patent/NZ583538A/en not_active IP Right Cessation
- 2008-09-15 CA CA2699718A patent/CA2699718C/en not_active Expired - Fee Related
- 2008-09-15 KR KR1020107008594A patent/KR101566042B1/en not_active IP Right Cessation
- 2008-09-15 CN CN2008801169950A patent/CN101868459B/en not_active Expired - Fee Related
- 2008-09-15 SI SI200830746T patent/SI2209778T1/en unknown
- 2008-09-15 PL PL08834504T patent/PL2209778T3/en unknown
- 2008-09-15 EA EA201000515A patent/EA019104B1/en not_active IP Right Cessation
- 2008-09-15 JP JP2010525902A patent/JP5722037B2/en not_active Expired - Fee Related
- 2008-09-15 DK DK08834504.6T patent/DK2209778T3/en active
- 2008-09-15 ES ES08834504T patent/ES2393824T3/en active Active
- 2008-09-15 UA UAA201004782A patent/UA101166C2/en unknown
- 2008-09-15 EP EP08834504A patent/EP2209778B1/en not_active Not-in-force
- 2008-09-15 ES ES13186328.4T patent/ES2569734T3/en active Active
- 2008-09-15 WO PCT/US2008/076401 patent/WO2009042435A1/en active Application Filing
- 2008-09-15 EP EP12181665A patent/EP2573087A1/en not_active Withdrawn
- 2008-09-15 EP EP16160414.5A patent/EP3078662A1/en not_active Withdrawn
- 2008-09-15 MX MX2010002772A patent/MX2010002772A/en active IP Right Grant
- 2008-09-15 US US12/678,995 patent/US8212045B2/en not_active Expired - Fee Related
- 2008-09-15 EP EP13186328.4A patent/EP2727910B1/en not_active Not-in-force
- 2008-09-19 AR ARP080104095A patent/AR068628A1/en not_active Application Discontinuation
- 2008-09-19 TW TW097136197A patent/TWI423799B/en not_active IP Right Cessation
-
2010
- 2010-03-02 IL IL204264A patent/IL204264A/en not_active IP Right Cessation
- 2010-03-04 TN TNP2010000100A patent/TN2010000100A1/en unknown
- 2010-03-29 ZA ZA2010/02206A patent/ZA201002206B/en unknown
- 2010-04-14 MA MA32775A patent/MA31779B1/en unknown
- 2010-04-21 CO CO10046631A patent/CO6270223A2/en not_active Application Discontinuation
- 2010-04-21 CR CR11383A patent/CR11383A/en unknown
- 2010-12-24 HK HK10112096.6A patent/HK1145498A1/en not_active IP Right Cessation
-
2011
- 2011-03-29 ZA ZA2011/02350A patent/ZA201102350B/en unknown
-
2012
- 2012-06-11 US US13/493,616 patent/US8853409B2/en not_active Expired - Fee Related
- 2012-10-11 HR HRP20120814AT patent/HRP20120814T1/en unknown
-
2014
- 2014-09-23 US US14/494,430 patent/US9079890B2/en not_active Expired - Fee Related
- 2014-11-06 HK HK14111244.5A patent/HK1197821A1/en not_active IP Right Cessation
-
2015
- 2015-03-12 CR CR20150131A patent/CR20150131A/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CO6270223A2 (en) | DERIVATIVES OF PIRIDIN-2-ILAMINO-1,2,4 TIADIAZOL AS GLUCOCINASE ACTIVATORS FOR THE TREATMENT OF MELLITUS DIABETES | |
ATE539748T1 (en) | GLUCOKINASE ACTIVATORS | |
SG170775A1 (en) | 2 -aminopyridine analogs as glucokinase activators | |
WO2008118718A3 (en) | 2-aminopyridine analogs as glucokinase activators | |
ATE521608T1 (en) | GLUCOKINASE ACTIVATORS | |
ECSP066894A (en) | DERIVATIVES OF SULFONAMIDE-THIAZOLPIRIDINE AS USEFUL GLUCOCINASE ACTIVATORS IN THE TREATMENT OF TYPE 2 DIABETES | |
TW200745037A (en) | Organic compounds | |
CO6410306A2 (en) | SGLT2 INHIBITOR TO TREAT MELLITUS DIABETES OF TYPE 1, MELLITUS DIABETES OF TYPE 2, ALTERATION OF TOLERANCE TO GLUCOSE AND HYPERGLUCEMIA | |
WO2010029089A3 (en) | Combination therapy for the treatment of diabetes and related conditions | |
EA201101187A1 (en) | ANTI-DIABETIC MEDICINES CONTAINING DPP-4 INHIBITOR (LINAGLIPTIN) OPTIONAL IN COMBINATION WITH OTHER ANTI-DIABETIC MEANS | |
MX2013004699A (en) | Pharmaceutical combinations for the treatment of metabolic disorders. | |
CR10976A (en) | 4-ARIL-1,4-DIHIDRO-1,6-NAFTIRIDINAMIDES REPLACED AND ITS USE | |
ECSP13012661A (en) | PHARMACEUTICAL COMPOSITION, TREATMENT METHODS AND USES OF THE SAME. | |
HK1130261A1 (en) | Bicyclic compounds and use as antidiabetics | |
WO2009055331A3 (en) | Bicyclic heterocycle derivatives and their use as modulators of the activity of gpr119 | |
CL2010001159A1 (en) | Compounds derived from 3,8-diazabicyclo [2.4.0] octane and 3,6-diazabicyclo [3.2.0] heptane disubstituted, orexin receptor modulators; pharmaceutical composition; Useful in the treatment of sleep disorders, metabolic disorders, among others. | |
UY32237A (en) | ARILO COMPOUNDS WITH HETEROCICLICAL SUBSTITUTES AND THEIR USE | |
GT200600011A (en) | PROCEDURES TO PREPARE ETERES OF PIRAZOLO [3,4-D] PYRIMIDINE | |
UY31803A (en) | CRYSTAL COMPOUND | |
MX2008011576A (en) | Substituted imidazo[2,1-b]thiazole compounds and their use for producing drugs. | |
CL2013000709A1 (en) | Composition containing nifurtimox and an anthelmintic selected from: pf1022, emopdepside, tribendimidine, amidantel, bay d 9216, praziquantel or benzyl benzoate; useful in the treatment of diseases caused by giardias (div. sol. 1577-10). | |
IL206738A0 (en) | Novel quinazoline-2,4-dione derivative, and medical compositions for the prophylaxis and treatment of cranial nerve disease containing the same | |
UY31352A1 (en) | GLUCOCINASE ACTIVATORS | |
WO2006076119A3 (en) | Treatment of skin diseases | |
CY1116557T1 (en) | PYRIDIN-2-YL-AMINO-1,2,4-THIADIAZOLI PRODUCTS AS GLYCOKINASE INHIBITORS FOR THE TREATMENT OF DIABETES |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Application refused |